Mazaki 2019 Biochem Biophys Res Commun: Difference between revisions

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Latest revision as of 17:32, 25 February 2020

Publications in the MiPMap
Mazaki Y, Takada S, Nio-Kobayashi J, Maekawa S, Higashi T, Onodera Y, Sabe H (2019) Mitofusin 2 is involved in chemotaxis of neutrophil-like differentiated HL-60โ€ฏcells. Biochem Biophys Res Commun 513:708-13.

ยป PMID: 30987827

Mazaki Y, Takada S, Nio-Kobayashi J, Maekawa S, Higashi T, Onodera Y, Sabe H (2019) Biochem Biophys Res Commun

Abstract: Neutrophils rapidly migrate to infection sites after the recognition of invaders. During chemotaxis, neutrophils require energy supplied by mitochondria oxidative phosphorylation (OXPHOS), whereas neutrophils rely heavily on glycolysis under normal conditions. Mitochondrial OXPHOS correlates with mitochondrial morphology. Here, we examined the mitochondrial morphology of neutrophil-like differentiated HL-60โ€ฏcells after chemoattractant N-formyl-Met-Leu-Phe (fMLP) stimulation. We found that mitochondrial morphology changes to a tubular form after fMLP stimulation. Mitochondrial OXPHOS activity and mitochondrial complex II significantly increased after fMLP stimulation. On the other hand, the silencing of mitochondrial fusion protein mitofusin 2 (MFN2) suppresses mitochondrial morphological changes. Furthermore, MFN2 silencing suppressed OXPHOS activation and chemotaxis after fMLP stimulation. These results suggest that MFN2 is involved in chemotaxis of differentiated HL-60โ€ฏcells depending on mitochondria.

Copyright ยฉ 2019 Elsevier Inc. All rights reserved. โ€ข Keywords: Chemotaxis, Mitofusin 2, Neutrophil, Oxidative phosphorylation โ€ข Bioblast editor: Plangger M โ€ข O2k-Network Lab: JP Sapporo Yokota T


Labels: MiParea: Respiration, mt-Structure;fission;fusion 


Organism: Human  Tissue;cell: Blood cells  Preparation: Permeabilized cells 


Coupling state: OXPHOS  Pathway: N, S  HRR: Oxygraph-2k 

Labels, 2019-04, JP 

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